How many (%) of th will have hemophili 8. Beta thalassemia is a blood disorder caused by a mutation the HBB gene on chromosome 11 which codes for the beta subunit of the hemoglobin protein. This changes the shape a functioning of the protein and causes it to misshapen and una to carry oxygen efficiently. The disorder is recessive. If two parents are carriers for the disorder, what percentage their children will have Beta Thalassemia? How many (%) o will have beta th Are males and fo equally? How d

Biology: The Unity and Diversity of Life (MindTap Course List)
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Chapter14: Chromosomes And Human Inheritance
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Problem 5GP: Human females have two X chromosomes (XX); males have one X and one Y chromosome (XY). a. With...
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How many (%) of their daughters
will have hemophilia?
8. Beta thalassemia is a blood disorder caused by a mutation in
the HBB gene on chromosome 11 which codes for the beta
subunit of the hemoglobin protein. This changes the shape and
functioning of the protein and causes it to misshapen and unable
to carry oxygen efficiently.
The disorder is recessive.
Normal
Beta thalassemia
If two parents are carriers for the disorder, what percentage of
their children will have Beta Thalassemia?
How many (%) of their children
will have beta thalassemia?
Are males and females affected
equally? How do you know?
Transcribed Image Text:How many (%) of their daughters will have hemophilia? 8. Beta thalassemia is a blood disorder caused by a mutation in the HBB gene on chromosome 11 which codes for the beta subunit of the hemoglobin protein. This changes the shape and functioning of the protein and causes it to misshapen and unable to carry oxygen efficiently. The disorder is recessive. Normal Beta thalassemia If two parents are carriers for the disorder, what percentage of their children will have Beta Thalassemia? How many (%) of their children will have beta thalassemia? Are males and females affected equally? How do you know?
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